Lista de obras -

A genetic association study of the FXYD domain containing ion transport regulator 6 (FXYD6) gene, encoding phosphohippolin, in susceptibility to schizophrenia in a Japanese population

artículo científico publicado en 2008

A genome-wide study reveals copy number variants exclusive to childhood obesity cases

artículo científico publicado en 2010

An association study of tachykinin receptor 3 gene with schizophrenia in the Japanese population.

artículo científico publicado en 2008

Analysis of a purported SHANK3 mutation in a boy with autism: clinical impact of rare variant research in neurodevelopmental disabilities

artículo científico publicado en 2010

Association analysis of the GDNF gene with methamphetamine use disorder in a Japanese population

artículo científico publicado en 2011

Association between chromogranin A gene polymorphism and schizophrenia in the Japanese population

artículo científico publicado en 2006

Association between gene polymorphisms of SLC22A3 and methamphetamine use disorder

artículo científico publicado en 2006

Association of Genetic Risks With Autism Spectrum Disorder and Early Neurodevelopmental Delays Among Children Without Intellectual Disability

artículo científico publicado en 2020

Association of SOX10 with schizophrenia in the Japanese population

artículo científico

Association study between vesicle-associated membrane protein 2 gene polymorphisms and fluvoxamine response in Japanese major depressive patients

artículo científico publicado en 2006

Common genetic variants on 5p14.1 associate with autism spectrum disorders

artículo científico publicado en 2009

Copy number variations in alternative splicing gene networks impact lifespan

artículo científico publicado en 2013

Extensive proteomic screening identifies the obesity-related NYGGF4 protein as a novel LRP1-interactor, showing reduced expression in early Alzheimer's disease

scientific journal article

Failure to replicate the association between NRG1 and schizophrenia using Japanese large sample

scientific article published on 20 February 2008

Gap junction coding genes and schizophrenia: a genetic association study

artículo científico publicado en 2007

Gene-wide association study between the methylenetetrahydrofolate reductase gene (MTHFR) and schizophrenia in the Japanese population, with an updated meta-analysis on currently available data

artículo científico publicado en 2010

Genetic analysis of the gene coding for DARPP-32 (PPP1R1B) in Japanese patients with schizophrenia or bipolar disorder

artículo científico publicado en 2007

Genome-wide copy number variation study associates metabotropic glutamate receptor gene networks with attention deficit hyperactivity disorder

artículo científico publicado en 2011

HDAC2 regulates atypical antipsychotic responses through the modulation of mGlu2 promoter activity.

artículo científico publicado en 2012

Haploinsufficiency of Cyfip1 produces fragile X-like phenotypes in mice

artículo científico publicado en 2012

Haploinsufficiency of Gtf2i, a gene deleted in Williams Syndrome, leads to increases in social interactions

artículo científico publicado en 2010

Haploinsufficiency of the autism-associated Shank3 gene leads to deficits in synaptic function, social interaction, and social communication

artículo científico publicado en 2010

Introduction of the human AVPR1A gene substantially alters brain receptor expression patterns and enhances aspects of social behavior in transgenic mice

artículo científico publicado en 2014

Linking oligodendrocyte and myelin dysfunction to neurocircuitry abnormalities in schizophrenia

scientific article published on 13 October 2010

Linking white and grey matter in schizophrenia: oligodendrocyte and neuron pathology in the prefrontal cortex

artículo científico publicado en 2009

Loss of function studies in mice and genetic association link receptor protein tyrosine phosphatase α to schizophrenia

artículo científico publicado en 2011

No association between tagging SNPs of SNARE complex genes (STX1A, VAMP2 and SNAP25) and schizophrenia in a Japanese population

artículo científico publicado en 2008

No association was found between a functional SNP in ZDHHC8 and schizophrenia in a Japanese case-control population

artículo científico publicado en 2004

Polygenic risk score analysis revealed shared genetic background in attention deficit hyperactivity disorder and narcolepsy

artículo científico publicado en 2020

Rare structural variation of synapse and neurotransmission genes in autism ⬇️

artículo científico publicado el 1 de marzo de 2011

Roles of glial cells in schizophrenia: Possible targets for therapeutic approaches ⬇️

artículo científico publicado el 9 de noviembre de 2012

Slc25a12 disruption alters myelination and neurofilaments: a model for a hypomyelination syndrome and childhood neurodevelopmental disorders

artículo científico publicado en 2009

Strong synaptic transmission impact by copy number variations in schizophrenia

artículo científico publicado en 2010

The 2',3'-cyclic nucleotide 3'-phosphodiesterase and oligodendrocyte lineage transcription factor 2 genes do not appear to be associated with schizophrenia in the Japanese population

artículo científico publicado en 2006

Lista de obras de

A genetic association study of the FXYD domain containing ion transport regulator 6 (FXYD6) gene, encoding phosphohippolin, in susceptibility to schizophrenia in a Japanese population

A genome-wide study reveals copy number variants exclusive to childhood obesity cases

An association study of tachykinin receptor 3 gene with schizophrenia in the Japanese population.

Analysis of a purported SHANK3 mutation in a boy with autism: clinical impact of rare variant research in neurodevelopmental disabilities

Association analysis of the GDNF gene with methamphetamine use disorder in a Japanese population

Association between chromogranin A gene polymorphism and schizophrenia in the Japanese population

Association between gene polymorphisms of SLC22A3 and methamphetamine use disorder

Association of Genetic Risks With Autism Spectrum Disorder and Early Neurodevelopmental Delays Among Children Without Intellectual Disability

Association of SOX10 with schizophrenia in the Japanese population

Association study between vesicle-associated membrane protein 2 gene polymorphisms and fluvoxamine response in Japanese major depressive patients

Common genetic variants on 5p14.1 associate with autism spectrum disorders

Copy number variations in alternative splicing gene networks impact lifespan

Extensive proteomic screening identifies the obesity-related NYGGF4 protein as a novel LRP1-interactor, showing reduced expression in early Alzheimer's disease

Failure to replicate the association between NRG1 and schizophrenia using Japanese large sample

Gap junction coding genes and schizophrenia: a genetic association study

Gene-wide association study between the methylenetetrahydrofolate reductase gene (MTHFR) and schizophrenia in the Japanese population, with an updated meta-analysis on currently available data

Genetic analysis of the gene coding for DARPP-32 (PPP1R1B) in Japanese patients with schizophrenia or bipolar disorder

Genome-wide copy number variation study associates metabotropic glutamate receptor gene networks with attention deficit hyperactivity disorder

HDAC2 regulates atypical antipsychotic responses through the modulation of mGlu2 promoter activity.

Haploinsufficiency of Cyfip1 produces fragile X-like phenotypes in mice

Haploinsufficiency of Gtf2i, a gene deleted in Williams Syndrome, leads to increases in social interactions

Haploinsufficiency of the autism-associated Shank3 gene leads to deficits in synaptic function, social interaction, and social communication

Introduction of the human AVPR1A gene substantially alters brain receptor expression patterns and enhances aspects of social behavior in transgenic mice

Linking oligodendrocyte and myelin dysfunction to neurocircuitry abnormalities in schizophrenia

Linking white and grey matter in schizophrenia: oligodendrocyte and neuron pathology in the prefrontal cortex

Loss of function studies in mice and genetic association link receptor protein tyrosine phosphatase α to schizophrenia

No association between tagging SNPs of SNARE complex genes (STX1A, VAMP2 and SNAP25) and schizophrenia in a Japanese population

No association was found between a functional SNP in ZDHHC8 and schizophrenia in a Japanese case-control population

Polygenic risk score analysis revealed shared genetic background in attention deficit hyperactivity disorder and narcolepsy

Rare structural variation of synapse and neurotransmission genes in autism ⬇️

Roles of glial cells in schizophrenia: Possible targets for therapeutic approaches ⬇️

Slc25a12 disruption alters myelination and neurofilaments: a model for a hypomyelination syndrome and childhood neurodevelopmental disorders

Strong synaptic transmission impact by copy number variations in schizophrenia

The 2',3'-cyclic nucleotide 3'-phosphodiesterase and oligodendrocyte lineage transcription factor 2 genes do not appear to be associated with schizophrenia in the Japanese population